Khegay Igor I, Popova Nelli A, Ivanova Ludmila N
Institute of Cytology and Genetics, Russian Academy of Sciences, Novosibirsk, Russia.
Tumour Biol. 2010 Dec;31(6):569-73. doi: 10.1007/s13277-010-0070-4. Epub 2010 Jun 18.
The growth pattern of carcinosarcoma Walker 256 was studied in rats with different levels of vasopressin in the blood. The Brattleboro rats are unable to synthesize vasopressin in a consequence of deletion in the coding gene. Hybrids from crossbreeding of the mutant Brattleboro and normal WAG rats inherit the one intact vasopressin gene and hold nearly normal hormone level. It was found that non-strain-specific carcinosarcoma Walker 256 intensively grows in WAG rats and their offsprings from crossbreeding with Brattleboro rats, and tumor development is equally terminated in them by death. Carcinosarcoma grows less intensely in Brattleboro rats; the tumor nodes increased only within the first 2 weeks, after which, the tumor began to decrease and eventually disappeared. Infusion of exogenous vasopressin to Brattleboro rats intensifies a tumor growth in the first 2 weeks after the inoculation of Walker 256 cells; however, it does not prevent a following regression and resorption of tumors.
研究了血液中血管加压素水平不同的大鼠体内沃克256癌肉瘤的生长模式。由于编码基因缺失,布拉特洛伯大鼠无法合成血管加压素。突变的布拉特洛伯大鼠与正常WAG大鼠杂交产生的杂种继承了一个完整的血管加压素基因,激素水平接近正常。研究发现,非品系特异性的沃克256癌肉瘤在WAG大鼠及其与布拉特洛伯大鼠杂交的后代中生长旺盛,肿瘤发展均以死亡告终。癌肉瘤在布拉特洛伯大鼠中的生长不那么旺盛;肿瘤结节仅在最初2周内增加,之后肿瘤开始缩小并最终消失。给布拉特洛伯大鼠注射外源性血管加压素会在接种沃克256细胞后的前2周内加剧肿瘤生长;然而,这并不能阻止随后肿瘤的消退和吸收。